HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylamine → alpha-Methoxyphenyl-hydroxy-cinnamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Methoxyphenylacetic acid | HCID 107202 | — |
| Product | alpha-Methoxyphenyl-hydroxy-cinnamic acid | HCID 70600588 | — |
Reaction Steps
Hydroxybenzaldehyde is mixed with methoxyphenylacetic acid and the resulting mixture is reacted with acetic anhydride and trimethylamine, to obtain α-methoxyphenyl-hydroxy-cinnamic acid. When this compound is acetylated by heating in a nitrogen gas atmosphere in the presence of quinoline and copper chromite, acetoxy-methoxy-stilbene is formed. Then, this stilbene derivative is catalytically reduced and hydrolyzed with an alkali to obtain 3-hydroxy-5 -methoxybibenzyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971651 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-076b9d2ad6ed4987ac3a79e2dc6df01e |
| Source note | uspto-grants-1976_07 |